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U Langenbeck

Showing results (31-40 of 68) with videos related to

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Biochimica Et Biophysica Acta|January 17, 1980
Characterization of experimental phenylketonuria. Augmentation of hyperphenylalaninemia with alpha-methylphenylalanine and p-chlorophenylalanineJ D Lane, B Schöne, U Langenbeck, et al.
Humangenetik|January 1, 1975
Heterozygote tests and genetic counseling in maple syrup urine disease: an application of Baye's theoremU Langenbeck, T Grimm, H W Rüdiger, et al.
European Journal of Pediatrics|November 1, 1982
Maple syrup urine disease--therapeutic use of insulin in catabolic statesU Wendel, U Langenbeck, I Lombeck, et al.
Pediatric Research|November 1, 1991
Oral L-alloisoleucine loading studies in healthy subjects and in patients with maple syrup urine diseaseP Schadewaldt, C Dalle-Feste, U Langenbeck, et al.
Journal of Mental Deficiency Research|September 1, 1986
Hyper-2-oxoglutaric aciduria in long-term mental handicapG Hoffmann, A Mench-Hoinowski, H Knüppel, et al.
American Journal of Medical Genetics|June 1, 1984
Developmental pathogenesis of chromosome disorders: report on two newly recognized signs of Down syndromeU Langenbeck, E Blum, C Wilkert-Walter, et al.
Biomedical Mass Spectrometry|August 1, 1977
Quinoxalinol derivatives of aliphatic 2-oxocarboxylic acids. Infrared and mass spectra of the O-trimethylsilylated compoundsU Langenbeck, H U Möhring, B Hinney, et al.
Journal of Inherited Metabolic Disease|October 26, 2006
Variant maple syrup urine disease (MSUD)--the entire spectrumE Simon, N Flaschker, P Schadewaldt, et al.
Human Genetics|January 1, 1984
Mean corpuscular hemoglobin is increased in Martin-Bell syndromeU Langenbeck, J Schmidtke, I Bartels, et al.
Hepatology (Baltimore, Md.)|July 1, 1984
Evidence for valine intolerance in patients with cirrhosisP Schauder, K Schröder, L Herbertz, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
Biochimica Et Biophysica Acta|January 17, 1980
Characterization of experimental phenylketonuria. Augmentation of hyperphenylalaninemia with alpha-methylphenylalanine and p-chlorophenylalanineJ D Lane, B Schöne, U Langenbeck, et al.
Humangenetik|January 1, 1975
Heterozygote tests and genetic counseling in maple syrup urine disease: an application of Baye's theoremU Langenbeck, T Grimm, H W Rüdiger, et al.
European Journal of Pediatrics|November 1, 1982
Maple syrup urine disease--therapeutic use of insulin in catabolic statesU Wendel, U Langenbeck, I Lombeck, et al.
Pediatric Research|November 1, 1991
Oral L-alloisoleucine loading studies in healthy subjects and in patients with maple syrup urine diseaseP Schadewaldt, C Dalle-Feste, U Langenbeck, et al.
Journal of Mental Deficiency Research|September 1, 1986
Hyper-2-oxoglutaric aciduria in long-term mental handicapG Hoffmann, A Mench-Hoinowski, H Knüppel, et al.
American Journal of Medical Genetics|June 1, 1984
Developmental pathogenesis of chromosome disorders: report on two newly recognized signs of Down syndromeU Langenbeck, E Blum, C Wilkert-Walter, et al.
Biomedical Mass Spectrometry|August 1, 1977
Quinoxalinol derivatives of aliphatic 2-oxocarboxylic acids. Infrared and mass spectra of the O-trimethylsilylated compoundsU Langenbeck, H U Möhring, B Hinney, et al.
Journal of Inherited Metabolic Disease|October 26, 2006
Variant maple syrup urine disease (MSUD)--the entire spectrumE Simon, N Flaschker, P Schadewaldt, et al.
Human Genetics|January 1, 1984
Mean corpuscular hemoglobin is increased in Martin-Bell syndromeU Langenbeck, J Schmidtke, I Bartels, et al.
Hepatology (Baltimore, Md.)|July 1, 1984
Evidence for valine intolerance in patients with cirrhosisP Schauder, K Schröder, L Herbertz, et al.
Pageof 7